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Merck
CN

RAWP02500

MF-Millipore膜滤器, 孔径1.2 µm

greener alternative

MF-Millipore, filter diam. 25 mm, hydrophilic

别名:

MCE膜过滤器,孔径1.2 μm

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UNSPSC Code:
40161507
NACRES:
NB.24
eCl@ss:
32031602
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产品名称

MF-Millipore膜滤器, 孔径1.2 µm, MF-Millipore, filter diam. 25 mm, hydrophilic

material

mixed cellulose esters (MCE) membrane
plain filter
white filter

agency

in accordance with NIOSH 7400,7402
in accordance with OSHA ID 160

description

25 mm diameter, mixed cellulose esters (MCE) membrane, hydrophilic, white, 100 discs

sterility

non-sterile

feature

hydrophilic

manufacturer/tradename

MF-Millipore
Millipore

sustainability

Greener Alternative Product

parameter

20 L/min-cm2 air flow rate
270 mL/min-cm2 water flow rate
75 °C max. temp.

diam.

25 mm

filter diam.

25 mm

thickness

150 μm

gravimetric extractables

5%

color

white

refractive index

n/D 1.512

matrix

MF-Millipore

pore size

1.2 μm pore size
82 % porosity

bubble point

≥0.76 bar, air with water at 23 °C

greener alternative category

shipped in

ambient

Quality Level

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Application

澄清水溶液

Features and Benefits

  • 适合生物和环境监控应用。
  • 可高压蒸汽灭菌,也可环氧乙烷灭菌和伽玛射线灭菌。

General description

MF-Millipore滤膜由生物惰性的醋酸纤维素和硝酸纤维素混合物组成,广泛用于各种研究和分析领域。
我们竭诚为您带来经过重新设计的绿色替代产品,实现可持续性更高的研究方案。滤膜的内盒&外盒均由遵循ISCC质量平衡分配的生物循环材料制成。 点击此处以获取更多信息。

Legal Information

MF-Millipore is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Flame

signalword

Danger

hcodes

Hazard Classifications

Flam. Sol. 1

存储类别

4.1B - Flammable solid hazardous materials

wgk

WGK 3


分析证书(COA)

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Werner Weitschies et al.
Journal of controlled release : official journal of the Controlled Release Society, 108(2-3), 375-385 (2005-10-11)
Gastrointestinal motility and transport as well as concomitant food intake are factors that are known to influence pharmacokinetics derived after intake of extended release dosage forms. However, the mechanisms behind these influencing factors are mostly unknown. In this study the
Claudiu V Giuraniuc et al.
PloS one, 8(5), e64419-e64419 (2013-05-16)
Construction of synthetic genetic networks requires the assembly of DNA fragments encoding functional biological parts in a defined order. Yet this may become a time-consuming procedure. To address this technical bottleneck, we have created a series of Gateway shuttle vectors

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